Human Phenotype Ontology 
Grandparent Node:
Neoplasm of striated muscle (HP:0009728)help
Grandparent Node:
Soft tissue sarcoma (HP:0030448)help
Parent Node:
Rhabdomyosarcoma (HP:0002859)help
..Starting node
Orbital rhabdomyosarcoma (HP:0500092)help
Term ID: 500092
Name: Orbital rhabdomyosarcoma
Definition: A mesenchymal tumour that is considered to be the commonest primary orbital malignancy in children. Histologically, it may be differentiated into embryonal, alveolar, and pleomorphic types. It is usually intraconal or within the superior orbit.
Reference: HP:0500092
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandAlveolar rhabdomyosarcoma (HP:0006779) help
..expandEmbryonal rhabdomyosarcoma (HP:0006743) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0500092HP:0500092Orbital rhabdomyosarcoma0 CL E G H

Genes (0) :

Diseases (0) :

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.